Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_002947 | 5402736 | 5402838 | 103 | 2 [1] | [1] 2 | hsdS | type I restriction modification system specificity protein |
CCTTATGCGAAAGCAGTTCTTGGGAGATACTCGAACCCTCGCCCAGCCAACATTAAATGTTGGCCTGATTCGTAGTGCCGCGGCACCTCTGCCTCCCCTCGCCGAACAACACCGCATCGTTGCCAAAGTCGAAGAAC > NC_002947/5402600‑5402736 | ccTTATGCGAAAGCAGTTCTTGGGAGATACTCGAACCCTCGCCCAGCCAACATTAAATGTTGGCCTGATTCGTAGTGCCGCGGCACCTCTGCCTCCCCTCGCCGAACAACACCGCATCGTTGCCAAAGTCgaagaa < 1:125879/136‑1 (MQ=255) cTTATGCGAAAGCAGTTCTTGGGAGATACTCGAACCCTCGCCCAGCCAACATTAAATGTTGGCCTGATTCGTAGTGCCGCGGCACCTCTGCCTCCCCTCGCCGAACAACACCGCATCGTTGCCAAAGTCGAAGAAc < 2:151573/136‑1 (MQ=255) | CCTTATGCGAAAGCAGTTCTTGGGAGATACTCGAACCCTCGCCCAGCCAACATTAAATGTTGGCCTGATTCGTAGTGCCGCGGCACCTCTGCCTCCCCTCGCCGAACAACACCGCATCGTTGCCAAAGTCGAAGAAC > NC_002947/5402600‑5402736 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |